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- NCIT_C142579 IAO_0000115 "A separate body such as an institutional, regional, national or supranational committee, made up of medical/scientific professionals and non-scientific members, whose responsibility it is to ensure the protection of the rights, safety, and well-being of human subjects involved in a clinical trial. It tries to provide public assurance of that protection by reviewing and approving the trial protocol, the suitability of the investigator(s), facilities, methods, and materials to be used in documenting informed consent of the trial subjects. (ICH)" @default.
- NCIT_C142579 NCIT_NHC0 "C142579" @default.
- NCIT_C142579 NCIT_P106 "Population Group" @default.
- NCIT_C142579 NCIT_P108 "Independent Ethics Committee" @default.
- NCIT_C142579 NCIT_P208 "CL540572" @default.
- NCIT_C142579 NCIT_P322 "CDISC" @default.
- NCIT_C142579 NCIT_P322 "CDISC-GLOSS" @default.
- NCIT_C142579 NCIT_P325 "An independent body (a review board or a committee, institutional, regional, national, or supranational) constituted of medical/scientific professionals and non-scientific members, whose responsibility it is to ensure the protection of the rights, safety, and well-being of human subjects involved in a trial and to provide public assurance of that protection by, among other things, reviewing and approving/providing favorable opinion on the trial protocol, the suitability of the investigator(s), facilities, and the methods and material to be used in obtaining and documenting informed consent of the trial subjects. NOTE: The legal status, composition, function, operations, and regulatory requirements pertaining to independent ethics committees may differ among countries but should allow the independent ethics committee to act in agreement with GCP as described in the ICH guideline. [After ICH E6 R2 Glossary] See also institutional review board, ethics committee." @default.
- NCIT_C142579 NCIT_P325 "An independent body (a review board or a committee, institutional, regional, national, or supranational), constituted of medical professionals and non-medical members, whose responsibility it is to ensure the protection of the rights, safety and well-being of human subjects involved in a study and to provide public assurance of that protection, by, among other things, reviewing and approving/providing favorable opinion on, the study protocol, the suitability of the investigator(s), facilities, and the methods and material to be used in obtaining and documenting informed consent of the study subjects. The legal status, composition, function, operations and regulatory requirements pertaining to Independent Ethics Committees may differ among countries, but should allow the Independent Ethics Committee to act in agreement with GCP as described in the ICH E6 guideline. (ICH E6 R2)" @default.
- NCIT_C142579 normalizedInformationContent "100" @default.
- NCIT_C142579 referenceCount "1" @default.
- NCIT_C142579 hasExactSynonym "IEC" @default.
- NCIT_C142579 hasExactSynonym "Independent Ethics Committee" @default.
- NCIT_C142579 hasExactSynonym "independent ethics committee (IEC)" @default.
- NCIT_C142579 inSubset NCIT_C132298 @default.
- NCIT_C142579 inSubset NCIT_C165642 @default.
- NCIT_C142579 inSubset NCIT_C61410 @default.
- NCIT_C142579 inSubset NCIT_C67497 @default.
- NCIT_C142579 type Class @default.
- NCIT_C142579 isDefinedBy ncit.owl @default.
- NCIT_C142579 label "Independent Ethics Committee" @default.
- NCIT_C142579 subClassOf NCIT_C142579 @default.
- NCIT_C142579 subClassOf NCIT_C17005 @default.
- NCIT_C142579 subClassOf NCIT_C199140 @default.
- NCIT_C142579 subClassOf NCIT_C20181 @default.
- NCIT_C142579 subClassOf NCIT_C43359 @default.
- NCIT_C142579 subClassOf NCIT_C78508 @default.